US20110300450A1

US20110300450A1 - Polyurethane gel electrolytes with improved conductance and/or solvent retention

Info

Publication number: US20110300450A1
Application number: US12/794,261
Authority: US
Inventors: Ramamurthy Balaji; Ajit R. Kulkarni; Raman S. Srinivasa
Original assignee: Indian Institute of Technology Bombay
Current assignee: Indian Institute of Technology Bombay
Priority date: 2010-06-04
Filing date: 2010-06-04
Publication date: 2011-12-08
Also published as: US8673503B2

Abstract

Disclosed are gel electrolytes comprising a polymer, which is a cross-linked polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound; a lithium salt; and a solvent, which is a carbonate solvent, a lactone solvent, or mixtures thereof.

Description

FIELD

The present disclosure provides a polyurethane (PU) based gel electrolyte having improved conductivity, high mechanical strength and high solvent retention.

BACKGROUND

A battery is a device that converts chemical energy into electrical energy by means of an electrochemical reaction. With the ever-increasing market for portable electronic devices, such as cell-phones, laptop computers, there is also an increased need for improved energy sources. Most of the electronic products today use “state-of-the-art” batteries, and yet the performance of these leaves much to be desired. Another aspect is the environmental threat posed by the heavy metals used in many of today's batteries. As society is becoming more aware of these problems, the desire for environmentally friendly battery components is growing.
Many of the electrical devices that consumers demand are limited by their power source. From electric vehicles to cellular phones, advances in battery technology have not kept pace with the power requirements of electrical devices. Lithium metal batteries have been targeted as the next generation power sources for these devices, since lithium has the most electropositive potential (−3.04 V versus standard hydrogen electrode), lowest equivalent weight (6.94 g/mol), lowest specific gravity (0.53 g/cm³) and highest mass ratio. These properties facilitate the design of storage systems with higher energy density compared with other battery systems.
A battery includes at least three main components: cathode, electrolyte and anode. The cathode is the electrode where a reduction reaction occurs, whereas the anode is the electrode where an oxidation reaction occurs. The electrolyte is an electronic insulator, but a good ionic conductor; one main function is to provide a transport medium from one electrode to the other. Although significant progress has been made in the development of batteries, several important factors, such as the electrolyte, have limited their commercial use.
Electrolytes should be chemically and electrochemically stable, mechanically strong, safe and inexpensive. Liquid electrolytes facilitate high-ionic mobility; however, due to safety concerns involving leakage and flammability, the use of liquid electrolytes in lithium battery systems has often been deterred. While solid electrolytes, such as ceramic and polymer electrolyte, prevent the formation of vapor-pressure and leakage problems, ionic transport within these materials is often too slow for typical battery applications. Ideally, an electrolyte would have the electrical properties of a liquid and the mechanical properties of a solid. Such an electrolyte would serve both as electrolyte and separator and provide the battery with mechanical flexibility, a property unattainable in cells with conventional liquid electrolytes.
Gel electrolytes possess both the cohesive properties of solids and the diffusive transport properties of liquids. This duality enables the gel to find a variety of important applications. Gels can be obtained as a result of either a chemical or a physical linking process. The use of substantial amounts of plasticizers in gel electrolyte gave rise to problems of mechanical strength and exudation of solvent which lead to thermal, chemical and electrochemical instability.

SUMMARY

Thus, in a broad aspect, the example embodiments provide polyurethane (PU) based gel electrolytes having one or more of improved conductivity, high mechanical strength and high solvent retention.
One aspect of the example embodiments provides a gel electrolyte including a polymer, wherein the polymer is a polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound; and the polymer is sufficiently cross-linked to form a gel in the presence of the solvent.
In another aspect, the illustrative embodiments provide a gel electrolyte comprising:
a polymer in about 20 to about 70 wt %;
a lithium salt in about 1 to about 8 wt %; and
a solvent comprising a carbonate solvent, a lactone solvent, or a mixture thereof;
wherein the polymer is a polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound; and the polymer is sufficiently cross-linked to form a gel in the presence of the solvent.
Another aspect of the embodiments provides a battery comprising any gel electrolyte of the embodiments.
Yet another aspect of the embodiments provides a method for preparing any gel electrolyte of the embodiments.
The foregoing summary is illustrative only and is not intended to be in any way limiting. In addition to the illustrative aspects, embodiments, and features described above, further aspects, embodiments, and features will become apparent by reference to the drawings and the following detailed description.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 illustrates XRD pattern of typical PU based gel electrolytes of an example embodiment; (a) is sample PU2_PC60 and (b) is sample PU2_PC35.

FIG. 2A illustrates an example SAXS pattern of sample PU2_PC40 and its liquid electrolyte.

FIG. 2B illustrates SAXS pattern of various PU electrolytes in an example embodiment.

FIG. 3 shows DSC patterns of PU gel based electrolytes with different solvent content.

FIG. 4A illustrates the temperature dependence of storage modulus in tensile mode at 1 Hz for PU gel electrolyte with varying PC content of an example embodiment.

FIG. 4B shows an example embodiment of the variation of the loss tangent (tan δ) at 1 Hz of PU gel electrolyte with temperature.

FIG. 5 illustrates the variation of Li⁺ conductivity at room temperature and activation energy with PC content in the PU gel electrolyte of an example embodiment.

FIG. 6 illustrates the Syneresis effect over time for PU gel electrolyte with varying PC content of an example embodiment.

DETAILED DESCRIPTION

In the following detailed description, reference is made to the accompanying drawings, which form a part hereof. In the drawings, similar symbols typically identify similar components, unless context dictates otherwise. The illustrative embodiments described in the detailed description, drawings, and claims are not meant to be limiting. Other embodiments may be utilized, and other changes may be made, without departing from the spirit or scope of the subject matter presented here. It will be readily understood that the aspects of the present disclosure, as generally described herein, and illustrated in the Figures, can be arranged, substituted, combined, and designed in a wide variety of different configurations, all of which are explicitly contemplated and are made part of this disclosure.
Thermoplastic polyurethane (PU) has limited capacity to contain solvents used in gel electrolytes; however, cross-linked PUs are known to hold more solvent and have higher lithium ion conductivities compared to thermoplastic PU. It is difficult to control the thickness of the cross-linked PU due to the random nature of the polymer reaction during the synthesis. The illustrative embodiments disclose a cross-linked PU based gel system where the thickness is controlled. The design of the gel is based on optimization of the electrical conductivity. The design is also based on optimization of the solvent exudation properties.
In one aspect, the disclosure provides a gel electrolyte including:
a polymer in about 20 to about 70 wt %;
a lithium salt in about 1 to about 8 wt. %; and
a solvent including a carbonate solvent, a lactone solvent, or a mixture thereof;
wherein the polymer is a polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound; and the polymer is sufficiently cross-linked to form a gel in the presence of the solvent.
Poly(alkyleneoxide) triols (PAO triols) selected from a wide range of molecular weights may be used in the methods of the examples. Unless otherwise defined, polymer molecular weights noted herein are weight-averaged molecular weights (M_W). Particular PAO triols useful in the example embodiments are those having molecular weights of from about 1,000 to about 100,000 g/mol. Some particular PAO triols have molecular weights from about 1,000 to about 50,000 g/mol. Other particular PAO triols have molecular weights from about 1,000 to about 10,000 g/mol. Some particular PAO triols have molecular weights from about 3,000 to about 7,000 g/mol. In still other embodiments, the molecular weight of the PAO triol is about 4,000 to about 5,000 g/mol. In still other embodiments, the molecular weight of the PAO triol is about 4,500 g/mol. In still other embodiments, the molecular weight of the PAO triol is less than 5,000 g/mol. Mixtures of PAO triols with different molecular weights can also be used.
In one example embodiment, the disclosure provides gel electrolyte as described above, wherein the poly(alkyleneoxide) triol is glycerin-type poly(alkyleneoxide).
In another embodiment, the disclosure provides gel electrolyte as described above, wherein the poly(alkyleneoxide) triol is glycerin-type poly(ethyleneoxide), glycerin-type poly(propyleneoxide), poly(ethyleneoxide) capped glycerin-type poly(propyleneoxide); and poly(propyleneoxide) capped glycerin-type poly(ethyleneoxide). Illustratively, the poly(alkyleneoxide) triol is selected from:
where m, n, and p are selected to form a polymer having molecular weight of about 1,000 to about 100,000 g/mol.
In one embodiment, the disclosure provides gel electrolyte as described above, wherein the poly(alkyleneoxide) triol is:
where m is selected to form a polymer having molecular weight of about 1,000 to about 100,000 g/mol.
In one embodiment, the disclosure provides gel electrolyte as described above, wherein the diisocyanate compound is selected from: methylenediphenyl diisocyante (MDI), p-phenylene diisocyante (PPDI), toluene diisocyanate (TDI), o-tolidine diisocyanate (TODD, xylylene diisocyanate (XDI), 1,5-naphthalene diisocyanate (NDI), 3,3′-dichloro-4,4′-diphenylmethane diisocyanate, hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), 4,4′-dicyclohexylmethane diisocyanate and hydrogenated xylylene diisocyanate. A mixture of two or more different diisocyanate compounds can also be used. In a particular embodiment, the diisocyanate compound is 4,4′-methylenediphenyl diisocyante (MDI).
In another embodiment, the diisocyanate compound of the disclosure is polymeric methylenediphenyl diisocyante (polymeric MDI). Example of polymeric MDI is SUPRASEC 2525 available from Huntsman, India. Polymeric MDI are selected from a wide range of molecular weights may be used in the methods of the example embodiment. Unless otherwise defined, polymers molecular weights noted herein are weight-averaged molecular weights (M_W). Particular polymeric MDI useful in the examples are those having molecular weights of from about 1,000 to 100,000 g/mol. Other particular polymeric MDI have molecular weights from about 1,000 to 10,000 g/mol. In still other embodiments, the molecular weight of the polymeric MDI is about 4,000 to 5,000 g/mol. In still other embodiments, the molecular weight of the polymeric MDI is about 4,500 g/mol. Mixtures of polymeric MDI with different molecular weights can also be used.
In another embodiment, the disclosure provides a gel electrolyte as described above wherein the polymer is in about 15 to about 75 wt %. In other embodiment, a gel electrolyte includes a polymer in about 25 to about 65 wt %. In another embodiment, a gel electrolyte has a polymer in about 30 to about 68 wt % In yet another embodiment, a gel electrolyte has a polymer in about 30 to about 55 wt %. In some embodiments, a gel electrolyte has a polymer in about 50 to about 65 wt %. In other embodiments, a gel electrolyte includes a polymer in about 40 to about 55 wt %. In yet another embodiment, a gel electrolyte has a polymer in about 30 to about 40 wt %. In yet another embodiment, a gel electrolyte includes a polymer in about 35 wt %.
Various lithium salts may be used in the methods of the example embodiment. For example, lithium salts include, but are not limited to lithium halides, lithium-metal salts, and other lithium compounds. Lithium halides include lithium bromide, lithium chloride, and lithium iodide. Lithium-metal salts include, but are not limited to lithium hexafluoroarsenate(V), and lithium hexafluorophosphate. Other lithium compounds include, but are not limited to bis(trifluoromethane)sulfonimide lithium salt, lithium borohydride, lithium dihydrogenphosphate, lithium tetrafluoroborate, lithium metaborate, lithium perchlorate, lithium thiophenolate, and lithium trifluoromethanesulfonate.
In one embodiment, the disclosure provides gel electrolyte as described above, wherein the lithium salt may include one or more of lithium perchlorate, lithium trifluoromethanesulfonate, lithium hexafluorophosphate, and lithium tetrafluoroborate.
In another embodiment, the disclosure provides gel electrolyte as described above, wherein the lithium salt is lithium perchlorate.
The disclosure also provides gel electrolyte as described above, wherein the lithium salt is present in about 2 to about 7 wt %. In some embodiments, the lithium salt is present in about 3 to about 6 wt %. In yet another embodiment, the lithium salt is present in about 5 to about 6 wt %. In yet another embodiment, the lithium salt is present in about 3 to about 5 wt %.
The disclosure also provides gel electrolyte as described above, wherein the lithium salt is present in about 1:15 to about 1:10 molar ratio relative to the solvent (i.e., the molar ratio of Li cation to the solvent is about 1:15). In some embodiments, the lithium salt is present in about 1:13 to about 1:11 molar ratio relative to the solvent. In yet another embodiment, the lithium salt is present in about 1:12 molar ratio relative to the solvent.
In a particular embodiment, the disclosure provides a gel electrolyte as described above wherein the solvent is the carbonate solvent. The carbonate solvent includes but is not limited to dimethyl carbonate, methyl ethyl carbonate, diethyl carbonate, dipropyl carbonate, dibutyl carbonate, propylene carbonate, ethylene carbonate, butylene carbonate, vinylene carbonate, and mixtures thereof.
In one embodiment, the disclosure provides gel electrolyte as described above, wherein the solvent is propylene carbonate, ethylene carbonate, or a mixture thereof. In a particular embodiment, the solvent is propylene carbonate. In another embodiment, the solvent is ethylene carbonate. In yet another embodiment, the disclosure provides gel electrolyte as described above, wherein the solvent is a mixture of propylene carbonate and ethylene carbonate in a 1:10; or 1:9; or 1:8; or 1:7; or 1:6; or 1:5; or 1:4; or 1:3; or 1:2; or 1:1: or 2:1; or 3:1; or 4:1; or 5:1; or 6:1; or 7:1; or 8:1; or 9:1 or 10:1 molar ratio. In yet another embodiment, the disclosure provides gel electrolyte as described above, wherein the solvent is a mixture of propylene carbonate and ethylene carbonate in a 1:1 molar ratio.
In a particular embodiment, the disclosure provides a gel electrolyte as described above wherein the solvent is the lactone solvent. The lactone solvent includes but is not limited to β-propiolactone, γ-butyrolactone, α-methyl-γ-butyrolactone, γ-crotonolactone, δ-valerolactone, γ-valerolactone, γ-caprolactone, ε-caprolactone, ethylated γ-butyrolactone, propylated γ-butyrolactone, and mixtures thereof.
In one embodiment, the disclosure provides gel electrolyte as described above, wherein the solvent is γ-butyrolactone.
In another embodiment, the disclosure provides gel electrolyte as described above, wherein the solvent is a mixture of the carbonate solvent and the lactone solvent. In a particular embodiment, the solvent is a mixture of propylene carbonate or ethylene carbonate, and γ-butyrolactone. In another embodiment, the solvent is a mixture of the carbonate solvent and the lactone solvent is in a 1:1 molar ratio.
In one embodiment, the disclosure provides gel electrolyte as described above, wherein the solvent is a mixture of propylene carbonate and γ-butyrolactone in a 1:1 molar ratio.
In another embodiment, the disclosure provides gel electrolyte as described above, wherein the solvent is a mixture of ethylene carbonate and γ-butyrolactone in a 1:1 molar ratio.
The disclosure also provides gel electrolyte as described above wherein poly(alkyleneoxide) triol and the diisocyanate compound are in about 1:1 to about 1.2:1 molar ratio. In one embodiment, the molar ratio of poly(alkyleneoxide) triol and the diisocyanate compound is about 1.1:1.
The disclosure provides gel electrolyte as described above including:
a polymer in about 30 to about 40 wt %;
a lithium salt in about 4 to about 5.5 wt. %; and
a solvent including a carbonate solvent, a lactone solvent, or a mixture thereof;
wherein the polymer is a polyurethane prepared from a poly(ethyleneoxide) triol and methylenediphenyl diisocyante (MDI) in a 1.1:1 molar ratio; and the polymer is sufficiently cross-linked to form a gel in the presence of the solvent. In this aspect, lithium salt, solvent, and solvent contents may be selected as described above for the preceding aspect of the example embodiments.
The disclosure also provides gel electrolyte as described above having:
a polymer in about 30 to about 40 wt %;
a lithium perchlorate in about 4 to about 5.5 wt. %; and
a solvent including a carbonate solvent, a lactone solvent, or a mixture thereof;
wherein the polymer is a polyurethane prepared from a poly(ethyleneoxide) triol and methylenediphenyl diisocyante (MDI) in a 1.1:1 molar ratio; and the polymer is sufficiently cross-linked to form a gel in the presence of the solvent.
The gel electrolytes of the disclosure can be used in a variety of applications, such as batteries, electrochemical capacitors, and electrochromic displays. Examples of electrochromic display devices or applications for which gel electrolytes can be particularly suitable include, but are not limited to helmets, mirrors, optical shutters, windows, glasses, goggles, color changeable eyewear, automotive windows, aircraft windows, welding visors or other devices that can change optical or electromagnetic transmission as a result of an applied potential. Additional examples include readable displays and super/ultra capacitors for power storage.
In a particular embodiment, the disclosure provides a battery comprising a gel electrolyte as described above.
The disclosure also provides method for preparing the gel electrolyte as described above. In a particular embodiment, the disclosure provides a method for preparing the gel electrolyte as described above, comprising:

- (a) adding a lithium salt to a solvent comprising a carbonate solvent, a lactone solvent, or a mixture thereof to form a liquid electrolyte; and
- (b) adding a polymer to the liquid electrolyte.

The cross-linking density of the polyurethanes prepared according to the methods described herein can be a function of a number of parameters which are familiar to those skilled in the art. For example, the cross-linking density can depend on one of more of: (1) the stoichiometric balance or imbalance of the alcohol and isocyanate reactive groups of the triol and diisocyanate, respectively; (2) the accessibility and/or reactivity of the individual end groups under the reaction conditions; and (3) the extent of the polymerization reaction between the triol and diisocyante, which can be controlled by changing the temperature and/or duration of the polymerization. The cross-linking density can be qualitatively analyzed using Dynamic Mechanical Analysis (DMA) and Small Angle X-ray Scattering (SAXS) measurements. The cross-linking density can be controlled, for example, by changing the molecular weight of PAO triol and/or the diisocyanate compound, or by changing the composition. The polyurethane of the disclosure should be sufficiently cross-linked to form a gel when mixed with or prepared in the presence of the solvent.

EXAMPLES

The preparation of the gel electrolytes of the disclosure is illustrated further by the following examples, which are not to be construed as limiting in scope or spirit to the specific procedures and gel electrolytes described in them.

General Procedure

Poly(ethylene oxide) triol (PEO triol) was purchased Korea Polyol Co. (KONIX FA 505) and has the average molecular weight of 4,500. Polymeric MDI was purchased from Huntsman, India (SUPRASEC 2525) and has the average molecular weight of 4,700. The gel electrolytes were prepared by solution casting technique. Conductivity was measured at room temperature using Novocontrol Alpha-N analyzer.

Example 1

PU-PC Based Gel Electrolyte

Propylene carbonate (PC) and lithium perchlorate (LiClO₄) were mixed in a molar ratio of 12:1. The liquid electrolyte was stirred at room temperature, and PEO triol (7.4 g) was introduced followed by MDI (1 g). The solution was mixed thoroughly and transferred to a polypropylene plate and kept at room temperature for 24 hours to complete the polymerization leading to the gel formation. The gel electrolytes thus obtained were kept in an oven at 50° C. for 12 hours to remove the excess solvent. The excess solvent lost in this step was estimated to be 1-3 wt %. Conductivity was measured at room temperature, and shown in Table 1. The weight percentages shown in Table 1 are prior to drying.
The polyurethane matrix with isocyanate to hydroxyl groups (NCO:OH) in 1:1 molar ratio for all the PC content shows non-homogeneity and micro phase separation. For the matrix with NCO:OH 1:1.2 molar ratio, uptake of PC content was limited to 45 wt %. Above this solvent content, gel electrolytes are not free standing and start flowing. The polyurethane matrix with NCO:OH 1:1.1 shows maximum of 60 wt % of PC uptake. The gelation time for this composition was about 10 hours. Increase in solvent content increases the conductivity of the gel electrolyte. At this ratio, the gels were homogenous and self standing.

	TABLE 1

	polymer	solvent

		con-		con-
	NCO:OH	tent		tent	LiClO₄
	molar	(wt	(molar	(wt	content	σDC at RT
Code	ratio	%)	ratio)	%)	(wt %)	(S/cm)

PU1_PC30	1:1	67.40	PC	30	2.60
PU1_PC33		64.14		33	2.86
PU1_PC35		61.96		35	3.03
PU1_PC40		56.53		40	3.47
PU1_PC45		51.10		45	3.90
PU1_PC50		45.67		50	4.33
PU1_PC55		40.28		55	4.77
PU1_PC60		34.80		60	5.20
PU1_PC65		29.37		65	5.63
PU2_PC30	1:1.1	67.40	PC	30	2.60
PU2_PC33		64.14		33	2.86	6.578 × 10⁻⁶
PU2_PC35		61.96		35	3.03	2.919 × 10⁻⁵
PU2_PC40		56.53		40	3.47	7.891 × 10⁻⁵
PU2_PC45		51.10		45	3.90	5.134 × 10⁻⁴
PU2_PC50		45.67		50	4.33	9.813 × 10⁻⁴
PU2_PC55		40.28		55	4.77	1.560 × 10⁻³
PU2_PC60		34.80		60	5.20	2.530 × 10⁻³
PU2_PC65		29.37		65	5.63
PU3_PC30	1:1.2	67.40	PC	30	2.60
PU3_PC33		64.14		33	2.86
PU3_PC35		61.96		35	3.03
PU3_PC40		56.53		40	3.47
PU3_PC45		51.10		45	3.90
PU3_PC50		45.67		50	4.33
PU3_PC55		40.28		55	4.77
PU3_PC60		34.80		60	5.20
PU3_PC65		29.37		65	5.63

Example 2

PU-γBL Based Gel Electrolyte

PU and γ-butyrolactone (γBL) based gel electrolyte was prepared essentially as described above. γBL and LiClO₄were mixed in a molar ratio of 12:1. Conductivity was measured at room temperature, and shown in Table 2.

Example 3

PU-Mixed Solvent Based Gel Electrolyte

PU with based gel electrolyte was prepared essentially as described above using PC-γBL, PC-ethylene carbonate (EC), and EC-γBL. The molar ratio of mixed solvents was fixed at 1:1; the molar ratio of the solvents to LiClO₄was fixed in a molar ratio of 12:1. Conductivity was measured at room temperature, and shown in Table 2. The weight percentages shown in Table 2 are prior to drying.

	TABLE 2

	polymer	solvent

		con-		con-
	NCO:OH	tent	(mo-	tent	LiClO₄
	molar	(wt	lar	(wt	content	σ_DCat RT
Code	ratio	%)	ratio)	%)	(wt %)	(S/cm)

PU2_γBL	1:1.1	33.84	γBL	60	6.16	1.80 × 10⁻³
PU2_PC_γBL		34.30	PC-	60	5.70	2.98 × 10⁻³
			γBL
			(1:1)
PU2_PC_EC		34.30	PC-	60	5.70	5.93 × 10⁻³
			EC
			(1:1)
PU2_EC_γBL		33.76	EC-	60	6.24	3.91 × 10⁻³
			γBL
			(1:1)

Results

The structure and morphology of the PU electrolytes have been studied by Wide Angle X-ray Diffraction (WAXD), Small Angle X-ray Scattering (SAXS), and SEM. The thermal properties of the PU electrolytes have been studied by Differential Scanning Calorimetry (DSC) and Dynamic Mechanical Analysis (DMA). The conductivity properties of the PU electrolytes have been studied by impedance spectroscopy. Different types of Li+ ions existing in these gels have been investigated by Li NMR, and their diffusivities were determined from pulsed field gradient experiments.

Wide Angle X-Ray Diffraction (WAXD):

The WAXD patterns for typical PU gels with 35 and 60 wt % propylene carbonate (PU2_PC35 and PU2_PC60) and are shown in FIG. 1. A weak and broad hump at 2θ value of ˜20° is seen in these patterns indicating the presence of an amorphous phase. Complete absence of sharp peaks indicates the absence of any crystalline phase in the gels. It may be noted that the WAXD patterns of other gels with various solvent content (33, 40, 45, 50, 55) were similar to the patterns in FIG. 1.

Small Angle X-Ray Scattering (SAXS):

FIG. 2( a) shows the typical SAXS pattern of a PU gel with 40 wt % propylene carbonate (PU2_PC40). The SAXS patterns were recorded up to 30 nm⁻¹. The SAXS pattern of polyurethane gel exhibits a broad hump and a strong peak at q value of ˜0.7 nm⁻¹and ˜14 nm⁻¹, respectively. The SAXS pattern of the liquid electrolyte also exhibits a strong peak at q value of ˜14 nm⁻¹, hence this peak seen in gel electrolyte is attributed to liquid electrolyte. The presence of broad hump at a q value of ˜0.7 nm⁻¹indicates the presence of two phase structure, hard segment (HS) and soft segment (SS), in polyurethane matrix. FIG. 2( b) shows the SAXS patterns of gels with different solvent contents in the range 35 to 60 wt %, where it's observed that increase in PC content leads to decrease in intensity of the peak with a slight shift towards lower q values. The height of this peak is also related to the number of crystallites (hard segments) per unit volume.

Differential Scanning Caloriemetry (DSC):

FIG. 3 shows DSC pattern of PU gel electrolytes with varying PC content (35, 40, 45, 50, 55 and 60 wt %). The results are also shown in Table 3. Without being limited to any one theory of operation, DSC studies indicated that there is no crystallization of PU based gel electrolytes.

TABLE 3

	PC	T_g(° C.)	T_g(° C.)
Code	(wt %)	(DSC)	(DMA)

PU2_PC33	33	−65	−47
PU2_PC35	35	−68	−49
PU2_PC40	40	−74	−52
PU2_PC45	45	−80	−54
PU2_PC50	50	−88	−58
PU2_PC55	55	−92	−64
PU2_PC60	60	−97	−70

Dynamic Mechanical Analysis (DMA):

FIG. 4A shows the temperature dependence of storage modulus in tensile mode for PU gel electrolyte with different PC content varying from 33 to 60 wt %, and FIG. 4B shows the variation of the loss tangent (tan δ) of PU gel electrolyte with temperature.

Ionic Conductivity:

FIG. 5 shows the variation of conductivity and activation energy with PC content in the gel. The activation energy of the gel electrolytes decreases with increase in PC content. Without being limited to any one theory of operation, lithium ion mobility was increased with fluidity of the gel (e.g., increased solvent content) and, as a result, increased the conductance. Morphological studies indicated that PU gel electrolyte is homogenous and free from pores.
The rate of solvent exudation with time in the gels was monitored by weight loss measurements. FIG. 6 shows a decrease in weight of the PU gel electrolytes with different PC content varying from 33 to 60 wt % over time. The decrease in weight is seen for all gels, and is attributed to the loss of solvent by exudation. PU gel with 33 wt % of PC solvent shows a loss of 1.5 wt % over 30 days and PU gel with 60 wt % PC solvent shows a loss of 3.5 wt % over the same period.
The present disclosure is not to be limited in terms of the particular embodiments described in this application, which are intended as illustrations of various aspects. Many modifications and variations can be made without departing from its spirit and scope, as will be apparent to those skilled in the art. Functionally equivalent methods and apparatuses within the scope of the disclosure, in addition to those enumerated herein, will be apparent to those skilled in the art from the foregoing descriptions. Such modifications and variations are intended to fall within the scope of the appended claims. The present disclosure is to be limited only by the terms of the appended claims, along with the full scope of equivalents to which such claims are entitled. It is to be understood that this disclosure is not limited to particular methods, reagents, compounds compositions or biological systems, which can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting.
With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth herein for sake of clarity.
It will be understood by those within the art that, in general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” the term “includes” should be interpreted as “includes but is not limited to,” etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim recitation to embodiments containing only one such recitation, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an” (e.g., “a” and/or “an” should be interpreted to mean “at least one” or “one or more”); the same holds true for the use of definite articles used to introduce claim recitations. In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should be interpreted to mean at least the recited number (e.g., the bare recitation of “two recitations,” without other modifiers, means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase “A or B” will be understood to include the possibilities of “A” or “B” or “A and B.”
In addition, where features or aspects of the disclosure are described in terms of Markush groups, those skilled in the art will recognize that the disclosure is also thereby described in terms of any individual member or subgroup of members of the Markush group.
As will be understood by one skilled in the art, for any and all purposes, such as in terms of providing a written description, all ranges disclosed herein also encompass any and all possible subranges and combinations of subranges thereof. Any listed range can be easily recognized as sufficiently describing and enabling the same range being broken down into at least equal halves, thirds, quarters, fifths, tenths, etc. As a non-limiting example, each range discussed herein can be readily broken down into a lower third, middle third and upper third, etc. As will also be understood by one skilled in the art all language such as “up to,” “at least,” “greater than,” “less than,” and the like include the number recited and refer to ranges which can be subsequently broken down into subranges as discussed above. Finally, as will be understood by one skilled in the art, a range includes each individual member. Thus, for example, a group having 1-3 cells refers to groups having 1, 2, or 3 cells. Similarly, a group having 1-5 cells refers to groups having 1, 2, 3, 4, or 5 cells, and so forth.
While various aspects and embodiments have been disclosed herein, other aspects and embodiments will be apparent to those skilled in the art. The various aspects and embodiments disclosed herein are for purposes of illustration and are not intended to be limiting, with the true scope and spirit being indicated by the following claims.

Claims

1. A gel electrolyte comprising:

a polymer in about 20 to about 70 wt %;

a lithium salt in about 1 to about 8 wt. %; and

a solvent comprising a carbonate solvent, a lactone solvent, or a mixture thereof;

wherein the polymer is a polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound; and the polymer is sufficiently cross-linked to form a gel in the presence of the solvent.

2. The gel electrolyte according to claim 1, wherein the poly(alkyleneoxide) triol comprises glycerin-type poly(alkyleneoxide).

3. The gel electrolyte according to claim 1, wherein the poly(alkyleneoxide) triol is selected from:

where m, n, and p are selected to form a polymer having molecular weight of about 1,000 to 100,000 g/mol.

4. The gel electrolyte according to claim 3, wherein the poly(alkyleneoxide) triol is

where m is selected to form a polymer having molecular weight of about 1,000 to 100,000 g/mol.

5. The gel electrolyte according to claim 1, wherein the diisocyanate compound is selected from: methylenediphenyl diisocyante (MDI), p-phenylene diisocyante (PPDI), toluene diisocyanate (TDI), o-tolidine diisocyanate (TODD, hexamethylene diisocyanate (HDI), and isophorone diisocyanate (IPDI).

6. The gel electrolyte according to claim 5, wherein the diisocyanate compound comprises 4,4′-methylenediphenyl diisocyante (MDI).

7. The gel electrolyte according to claim 1, wherein the polymer is present in about 25-50 wt %.

8. The gel electrolyte according to claim 1, wherein the polymer is present in about 35 wt %.

9. The gel electrolyte according to claim 1, wherein the lithium salt comprises lithium perchlorate.

10. The gel electrolyte according to claim 1, wherein the lithium salt is present in about 3-6 wt %.

11. The gel electrolyte according to claim 1, wherein the solvent comprises carbonate solvent.

12. The gel electrolyte according to claim 11, wherein the carbonate solvent comprises dimethyl carbonate, diethyl carbonate, propylene carbonate, ethylene carbonate, vinylene carbonate, or a mixture thereof.

13. The gel electrolyte according to claim 11, wherein the carbonate solvent comprises propylene carbonate, ethylene carbonate, or a mixture thereof.

14. The gel electrolyte according to claim 1, wherein the solvent comprises lactone solvent.

15. The gel electrolyte according to claim 14, wherein the lactone solvent comprises β-propiolactone, γ-butyrolactone, α-methyl-γ-butyrolactone, γ-crotonolactone, δ-valerolactone, γ-valerolactone, γ-caprolactone, ε-caprolactone, or mixtures thereof.

16. The gel electrolyte according to claim 14, wherein the lactone solvent comprises γ-butyrolactone.

17. The gel electrolyte according to claim 1, wherein the solvent comprises a mixture of the carbonate solvent and the lactone solvent.

18. The gel electrolyte according to claim 17, wherein the carbonate solvent comprises propylene carbonate or ethylene carbonate, and the lactone solvent is γ-butyrolactone.

19. A battery comprising the gel electrolyte according to claim 1.

20. A method for preparing the gel electrolyte according to claim 1.